GlaxoSmithKline, King of Prussia, PA, USA.
Vaccine. 2011 Nov 3;29(47):8483-6. doi: 10.1016/j.vaccine.2011.09.063. Epub 2011 Sep 25.
The duration of protection after vaccination with reduced antigen content diphtheria, tetanus and acellular pertussis vaccines (Tdap) is not known. Long-term post-vaccination serological data will help to improve understanding of the duration of humoral immunity and guide vaccination policy for the timing of repeat dose administration. The persistence of antibodies to Tdap antigens was measured 3 years after vaccination of adults 19-64 years of age with one of 2 Tdap vaccines (Boostrix(®), GlaxoSmithKline Biologicals; Tdap-B: or Adacel(®), Sanofi Pasteur; Tdap-A). In both groups, geometric mean concentrations for antibodies to diphtheria, tetanus, and pertussis vaccine antigens were decreased at year 3 relative to levels observed 1 month and 1 year following vaccination, but remained higher than pre-vaccination levels. Seroprotection rates for diphtheria and tetanus remained high for both Tdap vaccines (for diphtheria, 96.9% and 97.8% for the Tdap-B and Tdap-A groups, respectively; for tetanus, 98.1% and 99.6%, respectively).
接种低含量抗原白喉、破伤风和无细胞百日咳疫苗(Tdap)后的保护持续时间尚不清楚。长期疫苗接种后血清学数据将有助于更好地了解体液免疫的持续时间,并指导疫苗接种策略,以确定重复剂量给药的时间。在接种两种 Tdap 疫苗(Boostrix(®),葛兰素史克生物制品;Tdap-B 或 Adacel(®),赛诺菲巴斯德;Tdap-A)后 3 年,测量了 19-64 岁成年人的 Tdap 抗原抗体的持久性。与接种后 1 个月和 1 年相比,两组人群的白喉、破伤风和无细胞百日咳疫苗抗原抗体的几何平均浓度在第 3 年均有所下降,但仍高于接种前水平。两种 Tdap 疫苗的白喉和破伤风血清保护率均保持较高水平(Tdap-B 组和 Tdap-A 组的白喉血清保护率分别为 96.9%和 97.8%;破伤风血清保护率分别为 98.1%和 99.6%)。